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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Certain gene variants may raise the risk of prostate enlargement, but taking NSAIDs could reduce this risk.

Melatonin shortens the hair growth cycle by increasing PDGFA gene expression.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

The Agouti gene influences pigmentation and may have a developmental role in deer mice.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

The K14 promoter is more active in skin cells than the K5 promoter.

A new gene mutation is linked to monilethrix in the studied family.

Msx-2 gene removal speeds up skin wound healing in mice.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Black hairs have more pigment-related genes, while gray hairs have more keratin-related genes.

The hairless mutant gene causes early hair loss and affects skin and thymus development in mice.

Injecting specific oligonucleotides can change hair growth and structure by altering a gene.

The hr gene is linked to hair loss in Valle del Belice sheep.

PTCH gene mutations contribute to basal cell carcinoma development.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Mutations in the AR gene cause hair thinning and loss.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Certain gene variations are significantly linked to hair loss, especially in white people.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

New treatments targeting specific genes show promise for treating keratin disorders.